Dx | CC/MCC | Exclusions | Description |
P5221 | MCC | 1021:48 codes | Intraventricular (nontraumatic) hemorrhage, grade 3, of newborn |
P5222 | MCC | 1021:48 codes | Intraventricular (nontraumatic) hemorrhage, grade 4, of newborn |
P523 | CC | 1021:48 codes | Unspecified intraventricular (nontraumatic) hemorrhage of newborn |
P524 | MCC | 1020:39 codes | Intracerebral (nontraumatic) hemorrhage of newborn |
P525 | MCC | 1022:49 codes | Subarachnoid (nontraumatic) hemorrhage of newborn |
P526 | MCC | 1020:39 codes | Cerebellar (nontraumatic) and posterior fossa hemorrhage of newborn |
P528 | MCC | 1020:39 codes | Other intracranial (nontraumatic) hemorrhages of newborn |
P529 | MCC | 1020:39 codes | Intracranial (nontraumatic) hemorrhage of newborn, unspecified |
P53 | CC | 1035:28 codes | Hemorrhagic disease of newborn |
P541 | MCC | 1036:44 codes | Neonatal melena |
P542 | MCC | 1036:44 codes | Neonatal rectal hemorrhage |
P543 | MCC | 1036:44 codes | Other neonatal gastrointestinal hemorrhage |
P544 | CC | 1036:44 codes | Neonatal adrenal hemorrhage |
P560 | MCC | 1037:25 codes | Hydrops fetalis due to isoimmunization |
P5690 | MCC | 1037:25 codes | Hydrops fetalis due to unspecified hemolytic disease |
P5699 | MCC | 1037:25 codes | Hydrops fetalis due to other hemolytic disease |
P570 | MCC | 1037:25 codes | Kernicterus due to isoimmunization |
P578 | MCC | 1038:35 codes | Other specified kernicterus |
P579 | MCC | 1038:35 codes | Kernicterus, unspecified |
P591 | MCC | 1038:35 codes | Inspissated bile syndrome |
P5920 | MCC | 1038:35 codes | Neonatal jaundice from unspecified hepatocellular damage |
P5929 | MCC | 1038:35 codes | Neonatal jaundice from other hepatocellular damage |
P60 | MCC | 1035:28 codes | Disseminated intravascular coagulation of newborn |
P610 | MCC | 1035:28 codes | Transient neonatal thrombocytopenia |
P612 | CC | 1039:84 codes | Anemia of prematurity |
P613 | CC | 1039:84 codes | Congenital anemia from fetal blood loss |
P614 | CC | 1039:84 codes | Other congenital anemias, not elsewhere classified |
P615 | MCC | 1040:62 codes | Transient neonatal neutropenia |
P616 | CC | 1035:28 codes | Other transient neonatal disorders of coagulation |
P702 | CC | 1041:39 codes | Neonatal diabetes mellitus |
P708 | CC | 1042:22 codes | Other transitory disorders of carbohydrate metabolism of newborn |
P710 | CC | 1041:39 codes | Cow's milk hypocalcemia in newborn |
P711 | CC | 1041:39 codes | Other neonatal hypocalcemia |
P712 | CC | 1041:39 codes | Neonatal hypomagnesemia |
P713 | CC | 1041:39 codes | Neonatal tetany without calcium or magnesium deficiency |
P714 | CC | 1041:39 codes | Transitory neonatal hypoparathyroidism |
P718 | CC | 1041:39 codes | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | CC | 1041:39 codes | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P720 | CC | 1042:22 codes | Neonatal goiter, not elsewhere classified |
P721 | CC | 1041:39 codes | Transitory neonatal hyperthyroidism |
P722 | CC | 1042:22 codes | Other transitory neonatal disorders of thyroid function, not elsewhere classified |
P728 | CC | 1042:22 codes | Other specified transitory neonatal endocrine disorders |
P740 | MCC | 1041:39 codes | Late metabolic acidosis of newborn |
P745 | CC | 1042:22 codes | Transitory tyrosinemia of newborn |
P746 | CC | 1042:22 codes | Transitory hyperammonemia of newborn |
P748 | CC | 1042:22 codes | Other transitory metabolic disturbances of newborn |
P761 | CC | 1043:18 codes | Transitory ileus of newborn |
P771 | MCC | 1044:35 codes | Stage 1 necrotizing enterocolitis in newborn |
P772 | MCC | 1044:35 codes | Stage 2 necrotizing enterocolitis in newborn |
P773 | MCC | 1044:35 codes | Stage 3 necrotizing enterocolitis in newborn |
P779 | MCC | 1044:35 codes | Necrotizing enterocolitis in newborn, unspecified |
P780 | MCC | 1044:35 codes | Perinatal intestinal perforation |
P830 | CC | 1045:3 codes | Sclerema neonatorum |
P832 | MCC | 1046:18 codes | Hydrops fetalis not due to hemolytic disease |
P8330 | CC | 1047:9 codes | Unspecified edema specific to newborn |
P8339 | CC | 1047:9 codes | Other edema specific to newborn |
P90 | MCC | 1048:20 codes | Convulsions of newborn |
P910 | MCC | 1049:8 codes | Neonatal cerebral ischemia |
P911 | MCC | 1049:8 codes | Acquired periventricular cysts of newborn |
P912 | MCC | 1022:49 codes | Neonatal cerebral leukomalacia |
P913 | MCC | 1049:8 codes | Neonatal cerebral irritability |
P914 | MCC | 1049:8 codes | Neonatal cerebral depression |
P915 | MCC | 1049:8 codes | Neonatal coma |
P9160 | CC | 1050:5 codes | Hypoxic ischemic encephalopathy [HIE], unspecified |
P9161 | CC | 1050:5 codes | Mild hypoxic ischemic encephalopathy [HIE] |
P9162 | CC | 1050:5 codes | Moderate hypoxic ischemic encephalopathy [HIE] |
P9163 | MCC | 1050:5 codes | Severe hypoxic ischemic encephalopathy [HIE] |
P9201 | MCC | 1051:2 codes | Bilious vomiting of newborn |
P930 | CC | 1052:4 codes | Grey baby syndrome |
P938 | CC | 1052:4 codes | Other reactions and intoxications due to drugs administered to newborn |
P940 | CC | 1041:39 codes | Transient neonatal myasthenia gravis |
P961 | CC | 1052:4 codes | Neonatal withdrawal symptoms from maternal use of drugs of addiction |
P962 | CC | 1052:4 codes | Withdrawal symptoms from therapeutic use of drugs in newborn |
Q000 | MCC | 1053:3 codes | Anencephaly |
Q001 | MCC | 1053:3 codes | Craniorachischisis |
Q002 | MCC | 1053:3 codes | Iniencephaly |
Q010 | CC | 1054:14 codes | Frontal encephalocele |
Q011 | CC | 1054:14 codes | Nasofrontal encephalocele |
Q012 | CC | 1054:14 codes | Occipital encephalocele |
Q018 | CC | 1054:14 codes | Encephalocele of other sites |
Q019 | CC | 1054:14 codes | Encephalocele, unspecified |
Q040 | MCC | 1054:14 codes | Congenital malformations of corpus callosum |
Q041 | MCC | 1054:14 codes | Arhinencephaly |
Q042 | MCC | 1054:14 codes | Holoprosencephaly |
Q043 | MCC | 1054:14 codes | Other reduction deformities of brain |
Q044 | CC | 1055:4 codes | Septo-optic dysplasia of brain |
Q045 | CC | 1055:4 codes | Megalencephaly |
Q046 | CC | 1055:4 codes | Congenital cerebral cysts |
Q048 | CC | 1055:4 codes | Other specified congenital malformations of brain |
Q050 | CC | 1056:39 codes | Cervical spina bifida with hydrocephalus |
Q051 | CC | 1056:39 codes | Thoracic spina bifida with hydrocephalus |
Q052 | CC | 1056:39 codes | Lumbar spina bifida with hydrocephalus |
Q053 | CC | 1056:39 codes | Sacral spina bifida with hydrocephalus |
Q054 | CC | 1056:39 codes | Unspecified spina bifida with hydrocephalus |
Q0702 | CC | 1056:39 codes | Arnold-Chiari syndrome with hydrocephalus |
Q0703 | CC | 1056:39 codes | Arnold-Chiari syndrome with spina bifida and hydrocephalus |
Q200 | MCC | 1057:52 codes | Common arterial trunk |
Q201 | MCC | 1057:52 codes | Double outlet right ventricle |
Q202 | MCC | 1057:52 codes | Double outlet left ventricle |
Q203 | MCC | 1057:52 codes | Discordant ventriculoarterial connection |
Q204 | MCC | 1057:52 codes | Double inlet ventricle |
Q205 | CC | 1057:52 codes | Discordant atrioventricular connection |
Q210 | CC | 1057:52 codes | Ventricular septal defect |
Q211 | CC | 1058:43 codes | Atrial septal defect |
Q212 | CC | 1057:52 codes | Atrioventricular septal defect |
Q213 | MCC | 1057:52 codes | Tetralogy of Fallot |
Q220 | MCC | 1059:33 codes | Pulmonary valve atresia |
Q221 | CC | 1059:33 codes | Congenital pulmonary valve stenosis |
Q222 | CC | 1060:25 codes | Congenital pulmonary valve insufficiency |
Q223 | CC | 1060:25 codes | Other congenital malformations of pulmonary valve |
Q224 | MCC | 1061:39 codes | Congenital tricuspid stenosis |
Q225 | MCC | 1061:39 codes | Ebstein's anomaly |
Q226 | MCC | 1061:39 codes | Hypoplastic right heart syndrome |
Q228 | MCC | 1061:39 codes | Other congenital malformations of tricuspid valve |
Q229 | MCC | 1061:39 codes | Congenital malformation of tricuspid valve, unspecified |
Q230 | CC | 1061:39 codes | Congenital stenosis of aortic valve |
Q231 | CC | 1061:39 codes | Congenital insufficiency of aortic valve |
Q232 | CC | 1061:39 codes | Congenital mitral stenosis |
Q233 | CC | 1061:39 codes | Congenital mitral insufficiency |
Q234 | MCC | 1061:39 codes | Hypoplastic left heart syndrome |
Q240 | CC | 1062:26 codes | Dextrocardia |
Q241 | CC | 1062:26 codes | Levocardia |
Q242 | MCC | 1063:32 codes | Cor triatriatum |
Q243 | CC | 1063:32 codes | Pulmonary infundibular stenosis |
Q244 | MCC | 1063:32 codes | Congenital subaortic stenosis |
Q245 | CC | 1064:6 codes | Malformation of coronary vessels |
Q246 | MCC | 1065:30 codes | Congenital heart block |
Q250 | CC | 1066:6 codes | Patent ductus arteriosus |
Q251 | CC | 1067:20 codes | Coarctation of aorta |
Q2521 | CC | 1068:28 codes | Interruption of aortic arch |
Q2529 | CC | 1068:28 codes | Other atresia of aorta |
Q253 | CC | 1068:28 codes | Supravalvular aortic stenosis |
Q2540 | CC | 1069:32 codes | Congenital malformation of aorta unspecified |
Q2541 | CC | 1069:32 codes | Absence and aplasia of aorta |
Q2542 | CC | 1069:32 codes | Hypoplasia of aorta |
Q2543 | CC | 1069:32 codes | Congenital aneurysm of aorta |
Q2544 | CC | 1069:32 codes | Congenital dilation of aorta |
Q2545 | CC | 1069:32 codes | Double aortic arch |
Q2546 | CC | 1069:32 codes | Tortuous aortic arch |
Q2547 | CC | 1069:32 codes | Right aortic arch |
Q2548 | CC | 1069:32 codes | Anomalous origin of subclavian artery |
Q2549 | CC | 1069:32 codes | Other congenital malformations of aorta |
Q255 | MCC | 1070:11 codes | Atresia of pulmonary artery |
Q256 | MCC | 1070:11 codes | Stenosis of pulmonary artery |
Q2571 | MCC | 1070:11 codes | Coarctation of pulmonary artery |
Q2572 | MCC | 1070:11 codes | Congenital pulmonary arteriovenous malformation |
Q2579 | MCC | 1070:11 codes | Other congenital malformations of pulmonary artery |
Q258 | CC | 1069:32 codes | Other congenital malformations of other great arteries |
Q259 | CC | 1069:32 codes | Congenital malformation of great arteries, unspecified |
Q260 | CC | 1071:9 codes | Congenital stenosis of vena cava |
Q261 | CC | 1071:9 codes | Persistent left superior vena cava |
Q262 | CC | 1072:7 codes | Total anomalous pulmonary venous connection |
Q263 | CC | 1073:8 codes | Partial anomalous pulmonary venous connection |
Q264 | CC | 1073:8 codes | Anomalous pulmonary venous connection, unspecified |
Q268 | CC | 1071:9 codes | Other congenital malformations of great veins |
Q269 | CC | 1074:7 codes | Congenital malformation of great vein, unspecified |
Q2730 | CC | 1075:20 codes | Arteriovenous malformation, site unspecified |
Q274 | CC | 1075:20 codes | Congenital phlebectasia |
Q280 | CC | 1075:20 codes | Arteriovenous malformation of precerebral vessels |
Q281 | CC | 1075:20 codes | Other malformations of precerebral vessels |
Q282 | MCC | 1076:8 codes | Arteriovenous malformation of cerebral vessels |
Q283 | MCC | 1076:8 codes | Other malformations of cerebral vessels |
Q288 | CC | 1075:20 codes | Other specified congenital malformations of circulatory system |
Q289 | CC | 1077:90 codes | Congenital malformation of circulatory system, unspecified |
Q311 | CC | 1078:18 codes | Congenital subglottic stenosis |
Q312 | CC | 1078:18 codes | Laryngeal hypoplasia |
Q313 | CC | 1078:18 codes | Laryngocele |
Q315 | CC | 1078:18 codes | Congenital laryngomalacia |
Q318 | CC | 1078:18 codes | Other congenital malformations of larynx |
Q319 | CC | 1078:18 codes | Congenital malformation of larynx, unspecified |
Q320 | CC | 1078:18 codes | Congenital tracheomalacia |
Q321 | CC | 1078:18 codes | Other congenital malformations of trachea |
Q322 | CC | 1078:18 codes | Congenital bronchomalacia |
Q323 | CC | 1078:18 codes | Congenital stenosis of bronchus |
Q324 | CC | 1078:18 codes | Other congenital malformations of bronchus |
Q330 | CC | 1079:13 codes | Congenital cystic lung |
Q332 | MCC | 1079:13 codes | Sequestration of lung |
Q333 | MCC | 1079:13 codes | Agenesis of lung |
Q334 | CC | 1080:9 codes | Congenital bronchiectasis |
Q336 | MCC | 1079:13 codes | Congenital hypoplasia and dysplasia of lung |
Q390 | MCC | 1081:11 codes | Atresia of esophagus without fistula |
Q391 | MCC | 1081:11 codes | Atresia of esophagus with tracheo-esophageal fistula |
Q392 | MCC | 1081:11 codes | Congenital tracheo-esophageal fistula without atresia |
Q393 | MCC | 1081:11 codes | Congenital stenosis and stricture of esophagus |
Q394 | MCC | 1081:11 codes | Esophageal web |
Q395 | CC | 1082:6 codes | Congenital dilatation of esophagus |
Q396 | CC | 1082:6 codes | Congenital diverticulum of esophagus |
Q398 | CC | 1082:6 codes | Other congenital malformations of esophagus |
Q399 | CC | 1082:6 codes | Congenital malformation of esophagus, unspecified |
Q410 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of duodenum |
Q411 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of jejunum |
Q412 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of ileum |
Q418 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of other specified parts of small intestine |
Q419 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of small intestine, part unspecified |
Q420 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of rectum with fistula |
Q421 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of rectum without fistula |
Q422 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of anus with fistula |
Q423 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of anus without fistula |
Q428 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of other parts of large intestine |
Q429 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of large intestine, part unspecified |
Q431 | CC | 1085:4 codes | Hirschsprung's disease |
Q432 | CC | 1085:4 codes | Other congenital functional disorders of colon |
Q433 | CC | 1086:7 codes | Congenital malformations of intestinal fixation |
Q434 | CC | 1087:21 codes | Duplication of intestine |
Q435 | CC | 1087:21 codes | Ectopic anus |
Q436 | CC | 1087:21 codes | Congenital fistula of rectum and anus |
Q437 | CC | 1087:21 codes | Persistent cloaca |
Q438 | CC | 1087:21 codes | Other specified congenital malformations of intestine |
Q439 | CC | 1087:21 codes | Congenital malformation of intestine, unspecified |
Q440 | CC | 1088:8 codes | Agenesis, aplasia and hypoplasia of gallbladder |
Q441 | CC | 1088:8 codes | Other congenital malformations of gallbladder |
Q442 | MCC | 1089:4 codes | Atresia of bile ducts |
Q443 | MCC | 1089:4 codes | Congenital stenosis and stricture of bile ducts |
Q444 | CC | 1088:8 codes | Choledochal cyst |
Q445 | CC | 1088:8 codes | Other congenital malformations of bile ducts |
Q446 | CC | 1090:6 codes | Cystic disease of liver |
Q447 | CC | 1088:8 codes | Other congenital malformations of liver |
Q450 | CC | 1091:6 codes | Agenesis, aplasia and hypoplasia of pancreas |
Q451 | CC | 1091:6 codes | Annular pancreas |
Q452 | CC | 1091:6 codes | Congenital pancreatic cyst |
Q453 | CC | 1091:6 codes | Other congenital malformations of pancreas and pancreatic duct |
Q600 | CC | 1092:8 codes | Renal agenesis, unilateral |
Q601 | CC | 1092:8 codes | Renal agenesis, bilateral |
Q602 | CC | 1092:8 codes | Renal agenesis, unspecified |
Q603 | CC | 1092:8 codes | Renal hypoplasia, unilateral |
Q604 | CC | 1092:8 codes | Renal hypoplasia, bilateral |
Q605 | CC | 1092:8 codes | Renal hypoplasia, unspecified |
Q606 | CC | 1092:8 codes | Potter's syndrome |
Q6100 | CC | 1093:3 codes | Congenital renal cyst, unspecified |
Q6101 | CC | 1094:2 codes | Congenital single renal cyst |
Q6102 | CC | 1095:4 codes | Congenital multiple renal cysts |
Q6111 | CC | 1096:5 codes | Cystic dilatation of collecting ducts |
Q6119 | CC | 1096:5 codes | Other polycystic kidney, infantile type |
Q612 | CC | 1096:5 codes | Polycystic kidney, adult type |
Q613 | CC | 1096:5 codes | Polycystic kidney, unspecified |
Q614 | CC | 1097:2 codes | Renal dysplasia |
Q615 | CC | 1095:4 codes | Medullary cystic kidney |
Q618 | CC | 1095:4 codes | Other cystic kidney diseases |
Q619 | CC | 1093:3 codes | Cystic kidney disease, unspecified |
Q620 | CC | 1098:7 codes | Congenital hydronephrosis |
Q6210 | CC | 1098:7 codes | Congenital occlusion of ureter, unspecified |
Q6211 | CC | 1098:7 codes | Congenital occlusion of ureteropelvic junction |
Q6212 | CC | 1098:7 codes | Congenital occlusion of ureterovesical orifice |
Q622 | CC | 1098:7 codes | Congenital megaureter |
Q6231 | CC | 1098:7 codes | Congenital ureterocele, orthotopic |
Q6232 | CC | 1098:7 codes | Cecoureterocele |
Q6239 | CC | 1098:7 codes | Other obstructive defects of renal pelvis and ureter |
Q6410 | CC | 1099:7 codes | Exstrophy of urinary bladder, unspecified |
Q6411 | CC | 1099:7 codes | Supravesical fissure of urinary bladder |
Q6412 | CC | 1099:7 codes | Cloacal extrophy of urinary bladder |
Q6419 | CC | 1099:7 codes | Other exstrophy of urinary bladder |
Q642 | CC | 1100:8 codes | Congenital posterior urethral valves |
Q6431 | CC | 1100:8 codes | Congenital bladder neck obstruction |
Q6432 | CC | 1100:8 codes | Congenital stricture of urethra |
Q6433 | CC | 1100:8 codes | Congenital stricture of urinary meatus |
Q6439 | CC | 1100:8 codes | Other atresia and stenosis of urethra and bladder neck |
Q675 | CC | 1101:7 codes | Congenital deformity of spine |
Q678 | CC | 1102:5 codes | Other congenital deformities of chest |
Q681 | CC | 1102:5 codes | Congenital deformity of finger(s) and hand |
Q743 | CC | 1102:5 codes | Arthrogryposis multiplex congenita |
Q763 | CC | 1101:7 codes | Congenital scoliosis due to congenital bony malformation |
Q76425 | CC | 1101:7 codes | Congenital lordosis, thoracolumbar region |
Q76426 | CC | 1101:7 codes | Congenital lordosis, lumbar region |
Q76427 | CC | 1101:7 codes | Congenital lordosis, lumbosacral region |
Q76428 | CC | 1101:7 codes | Congenital lordosis, sacral and sacrococcygeal region |
Q76429 | CC | 1101:7 codes | Congenital lordosis, unspecified region |
Q766 | CC | 1103:6 codes | Other congenital malformations of ribs |
Q767 | CC | 1103:6 codes | Congenital malformation of sternum |
Q768 | CC | 1103:6 codes | Other congenital malformations of bony thorax |
Q769 | CC | 1103:6 codes | Congenital malformation of bony thorax, unspecified |
Q772 | CC | 1103:6 codes | Short rib syndrome |
Q780 | CC | 1104:10 codes | Osteogenesis imperfecta |
Q782 | CC | 1104:10 codes | Osteopetrosis |
Q790 | MCC | 1105:3 codes | Congenital diaphragmatic hernia |
Q791 | MCC | 1105:3 codes | Other congenital malformations of diaphragm |
Q792 | MCC | 1106:5 codes | Exomphalos |
Q793 | MCC | 1106:5 codes | Gastroschisis |
Q794 | MCC | 1106:5 codes | Prune belly syndrome |
Q7951 | MCC | 1106:5 codes | Congenital hernia of bladder |
Q7959 | MCC | 1106:5 codes | Other congenital malformations of abdominal wall |
Q796 | CC | 1107:1 code | Ehlers-Danlos syndrome |
Q851 | CC | 1108:5 codes | Tuberous sclerosis |
Q858 | CC | 1109:3 codes | Other phakomatoses, not elsewhere classified |
Q859 | CC | 1109:3 codes | Phakomatosis, unspecified |
Q871 | CC | 1110:20 codes | Congenital malformation syndromes predominantly associated with short stature |
Q872 | CC | 0540:16 codes | Congenital malformation syndromes predominantly involving limbs |
Q873 | CC | 0540:16 codes | Congenital malformation syndromes involving early overgrowth |
Q8740 | CC | 1110:20 codes | Marfan's syndrome, unspecified |
Q87410 | CC | 1110:20 codes | Marfan's syndrome with aortic dilation |
Q87418 | CC | 1110:20 codes | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | CC | 1110:20 codes | Marfan's syndrome with ocular manifestations |
Q8743 | CC | 1110:20 codes | Marfan's syndrome with skeletal manifestation |
Q875 | CC | 0540:16 codes | Other congenital malformation syndromes with other skeletal changes |
Q8781 | CC | 0540:16 codes | Alport syndrome |
Q8782 | CC | 0540:16 codes | Arterial tortuosity syndrome |
Q8789 | CC | 0540:16 codes | Other specified congenital malformation syndromes, not elsewhere classified |
Q8901 | CC | 1111:3 codes | Asplenia (congenital) |
Q8909 | CC | 1111:3 codes | Congenital malformations of spleen |
Q893 | CC | 1112:3 codes | Situs inversus |
Q894 | MCC | 1113:3 codes | Conjoined twins |
Q897 | CC | 1112:3 codes | Multiple congenital malformations, not elsewhere classified |
Q898 | CC | 0540:16 codes | Other specified congenital malformations |
Q910 | CC | 1114:65 codes | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
Q911 | CC | 1114:65 codes | Trisomy 18, mosaicism (mitotic nondisjunction) |
Q912 | CC | 1114:65 codes | Trisomy 18, translocation |
Q913 | CC | 1114:65 codes | Trisomy 18, unspecified |
Q914 | CC | 1114:65 codes | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
Q915 | CC | 1114:65 codes | Trisomy 13, mosaicism (mitotic nondisjunction) |
Q916 | CC | 1114:65 codes | Trisomy 13, translocation |
Q917 | CC | 1114:65 codes | Trisomy 13, unspecified |
Q933 | CC | 1115:60 codes | Deletion of short arm of chromosome 4 |
Q934 | CC | 1116:64 codes | Deletion of short arm of chromosome 5 |
Q935 | CC | 1115:60 codes | Other deletions of part of a chromosome |
Q937 | CC | 1115:60 codes | Deletions with other complex rearrangements |
Q9381 | MCC | 1117:64 codes | Velo-cardio-facial syndrome |
Q9388 | CC | 1118:64 codes | Other microdeletions |
Q9389 | CC | 1115:60 codes | Other deletions from the autosomes |
Q939 | CC | 1115:60 codes | Deletion from autosomes, unspecified |
R042 | CC | 1119:6 codes | Hemoptysis |
R0481 | CC | 1119:6 codes | Acute idiopathic pulmonary hemorrhage in infants |
R0489 | CC | 1119:6 codes | Hemorrhage from other sites in respiratory passages |
R049 | CC | 1119:6 codes | Hemorrhage from respiratory passages, unspecified |
R063 | CC | 1120:19 codes | Periodic breathing |
R0901 | CC | 1121:100 codes | Asphyxia |
R092 | MCC | 1121:100 codes | Respiratory arrest |
R17 | CC | 1122:21 codes | Unspecified jaundice |
R180 | CC | 1123:103 codes | Malignant ascites |
R188 | CC | 1123:103 codes | Other ascites |
R290 | CC | 1124:140 codes | Tetany |
R291 | CC | 1125:2 codes | Meningismus |
R295 | CC | 1126:2 codes | Transient paralysis |
R390 | CC | 1127:7 codes | Extravasation of urine |
R4020 | MCC | 0515:841 codes | Unspecified coma |
R402110 | MCC | 0515:841 codes | Coma scale, eyes open, never, unspecified time |
R402111 | MCC | 0515:841 codes | Coma scale, eyes open, never, in the field [EMT or ambulance] |
R402112 | MCC | 0515:841 codes | Coma scale, eyes open, never, at arrival to emergency department |
R402113 | MCC | 0515:841 codes | Coma scale, eyes open, never, at hospital admission |
R402114 | MCC | 0515:841 codes | Coma scale, eyes open, never, 24 hours or more after hospital admission |
R402120 | MCC | 0515:841 codes | Coma scale, eyes open, to pain, unspecified time |
R402121 | MCC | 0515:841 codes | Coma scale, eyes open, to pain, in the field [EMT or ambulance] |
R402122 | MCC | 0515:841 codes | Coma scale, eyes open, to pain, at arrival to emergency department |
R402123 | MCC | 0515:841 codes | Coma scale, eyes open, to pain, at hospital admission |
R402124 | MCC | 0515:841 codes | Coma scale, eyes open, to pain, 24 hours or more after hospital admission |
R402210 | MCC | 0515:841 codes | Coma scale, best verbal response, none, unspecified time |
R402211 | MCC | 0515:841 codes | Coma scale, best verbal response, none, in the field [EMT or ambulance] |
R402212 | MCC | 0515:841 codes | Coma scale, best verbal response, none, at arrival to emergency department |
R402213 | MCC | 0515:841 codes | Coma scale, best verbal response, none, at hospital admission |
R402214 | MCC | 0515:841 codes | Coma scale, best verbal response, none, 24 hours or more after hospital admission |
R402220 | MCC | 0515:841 codes | Coma scale, best verbal response, incomprehensible words, unspecified time |
R402221 | MCC | 0515:841 codes | Coma scale, best verbal response, incomprehensible words, in the field [EMT or ambulance] |
R402222 | MCC | 0515:841 codes | Coma scale, best verbal response, incomprehensible words, at arrival to emergency department |
R402223 | MCC | 0515:841 codes | Coma scale, best verbal response, incomprehensible words, at hospital admission |
R402224 | MCC | 0515:841 codes | Coma scale, best verbal response, incomprehensible words, 24 hours or more after hospital admission |
R402310 | MCC | 0515:841 codes | Coma scale, best motor response, none, unspecified time |
R402311 | MCC | 0515:841 codes | Coma scale, best motor response, none, in the field [EMT or ambulance] |
R402312 | MCC | 0515:841 codes | Coma scale, best motor response, none, at arrival to emergency department |
R402313 | MCC | 0515:841 codes | Coma scale, best motor response, none, at hospital admission |
R402314 | MCC | 0515:841 codes | Coma scale, best motor response, none, 24 hours or more after hospital admission |
R402320 | MCC | 0515:841 codes | Coma scale, best motor response, extension, unspecified time |
R402321 | MCC | 0515:841 codes | Coma scale, best motor response, extension, in the field [EMT or ambulance] |
R402322 | MCC | 0515:841 codes | Coma scale, best motor response, extension, at arrival to emergency department |
R402323 | MCC | 0515:841 codes | Coma scale, best motor response, extension, at hospital admission |
R402324 | MCC | 0515:841 codes | Coma scale, best motor response, extension, 24 hours or more after hospital admission |
R402340 | MCC | 0515:841 codes | Coma scale, best motor response, flexion withdrawal, unspecified time |
R402341 | MCC | 0515:841 codes | Coma scale, best motor response, flexion withdrawal, in the field [EMT or ambulance] |
R402342 | MCC | 0515:841 codes | Coma scale, best motor response, flexion withdrawal, at arrival to emergency department |
R402343 | MCC | 0515:841 codes | Coma scale, best motor response, flexion withdrawal, at hospital admission |
R402344 | MCC | 0515:841 codes | Coma scale, best motor response, flexion withdrawal, 24 hours or more after hospital admission |
R403 | CC | 0515:841 codes | Persistent vegetative state |
R414 | CC | 1128:8 codes | Neurologic neglect syndrome |
R440 | CC | 1129:88 codes | Auditory hallucinations |
R442 | CC | 1129:88 codes | Other hallucinations |
R443 | CC | 1129:88 codes | Hallucinations, unspecified |
R45851 | CC | 1130:1 code | Suicidal ideations |
R4701 | CC | 1131:137 codes | Aphasia |
R532 | MCC | 0595:155 codes | Functional quadriplegia |
R5600 | CC | 1132:147 codes | Simple febrile convulsions |
R5601 | CC | 1132:147 codes | Complex febrile convulsions |
R561 | CC | 0582:87 codes | Post traumatic seizures |
R570 | MCC | 1133:90 codes | Cardiogenic shock |
R571 | MCC | 1133:90 codes | Hypovolemic shock |
R578 | MCC | 1133:90 codes | Other shock |
R579 | CC | 1133:90 codes | Shock, unspecified |
R64 | CC | 1134:85 codes | Cachexia |
R6510 | CC | 0071:91 codes | Systemic inflammatory response syndrome (SIRS) of non-infectious origin without acute organ dysfunction |
R6511 | MCC | 0071:91 codes | Systemic inflammatory response syndrome (SIRS) of non-infectious origin with acute organ dysfunction |
R6520 | MCC | 0071:91 codes | Severe sepsis without septic shock |
R6521 | MCC | 1133:90 codes | Severe sepsis with septic shock |
R710 | CC | 1135:5 codes | Precipitous drop in hematocrit |
R7881 | CC | 1136:106 codes | Bacteremia |
R820 | CC | 1137:93 codes | Chyluria |
R821 | CC | 1138:94 codes | Myoglobinuria |
S01101A | CC | 1139:55 codes | Unspecified open wound of right eyelid and periocular area, initial encounter |
S01102A | CC | 1139:55 codes | Unspecified open wound of left eyelid and periocular area, initial encounter |
S01109A | CC | 1139:55 codes | Unspecified open wound of unspecified eyelid and periocular area, initial encounter |
S020XXA | CC | 1140:335 codes | Fracture of vault of skull, initial encounter for closed fracture |
S020XXB | MCC | 1140:335 codes | Fracture of vault of skull, initial encounter for open fracture |
S020XXK | CC | 0897:5,551 codes | Fracture of vault of skull, subsequent encounter for fracture with nonunion |
S02101A | CC | 1140:335 codes | Fracture of base of skull, right side, initial encounter for closed fracture |
S02101B | MCC | 1140:335 codes | Fracture of base of skull, right side, initial encounter for open fracture |